Ajanta Pharma-interview for Quality Control on 16th June 2024@ Dehradun

Ajanta Pharma-interview for Quality Control on 16th June 2024@ Dehradun

Ajanta Pharma-interview

WALK-IN-INTERVIEW AT DEHRADUN
ap ajanta pharma
Ajanta Pharma Limited, a specialty Pharmaceutical company engaged in development, manufacture and marketing of quality finished dosage in domestic and international markets is looking for suitable candidates for its formulation facility at Guwahati, Assam.
Quality Control -Sr. Officer/Officer
• Qualification-M.Pharma/B.Pharma/ MSc/BSc.
• Experience:02 to 07 Years
Job Description

• Method transfer of Pharmaceuticals Products and Materials.
⚫ Analysis of in-process, Finished products and Stability study samples.
• Sampling and testing of Raw Materials, Packaging Materials and Water samples.
• Calibration and Handling of Laboratory Instruments like GC, HPLC and Autotitrator etc.
• Preparation, Qualification and Handling of Working standard, Reference standard and Primary Standard.
• Preparation and standardization of Volumetric Solution and Regent.
Basic Knowledge on laboratory OOS, OOT and Incident.
Interested candidates from pharma formulation manufacturing plant may attend walk-in-interview with the copy of their latest Resume, CTC Break up and passport size photograph on

Date: June 16th, 2024(Sunday)
Time 09:00 am to 06:00 pm
Venue: The Competant Palace, Chakrata Road, Selaqui Industrial Area, Central Hope Town, Selaqui,Dehradun-97

Contact: Sahil Sinha/8927316680
*Note:Preference shall be given to the candidates who are resident of Assam
Candidates those are unable to attend the Walk-In-Interview may share their resume on sahilinha@ajantapharma.com

Job Category: pharma
Job Type: Full Time
Job Location: Selaqui

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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